NM_001378030.1(CCDC78):c.1053+18C>T AND Congenital myopathy with internal nuclei and atypical cores
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003534162.1
Allele description [Variation Report for NM_001378030.1(CCDC78):c.1053+18C>T]
NM_001378030.1(CCDC78):c.1053+18C>T
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024